Canonical Allele Identifier: CA1806686199

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102232163A= , CM000670.2:g.102232163A=	GRCh38
NC_000008.10:g.103244391A= , CM000670.1:g.103244391A=	GRCh37
NC_000008.9:g.103313567A=	NCBI36
NG_016617.1:g.11956T= , LRG_788:g.11956T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000251810.8:c.190T= MANE Select	ENSP00000251810.3:p.Trp64=
ENST00000251810.7:c.190T=	ENSP00000251810.3:p.Trp64=
ENST00000395912.6:c.49-6129T=	ENSP00000379248.2:n.49-6129T=
ENST00000517517.1:n.499T=
ENST00000519317.5:c.48+6664T=	ENSP00000430641.1:n.48+6664T=
ENST00000519962.5:c.48+6664T=	ENSP00000429140.1:n.48+6664T=
ENST00000522368.5:c.359T=
ENST00000522394.1:c.122+68T=	ENSP00000429578.1:n.122+68T=
ENST00000523957.1:c.*113T=	ENSP00000427830.1:n.*113T=
ENST00000621845.1:c.28T=	ENSP00000484318.1:p.Trp10=
NM_001172477.1:c.406T= , LRG_788t1:c.406T=	NP_001165948.1:p.Trp136=
NM_001172478.1:c.49-6129T=	NP_001165949.1:n.49-6129T=
NM_015713.4:c.190T= , LRG_788t2:c.190T=	NP_056528.2:p.Trp64=
NM_001172478.2:c.49-6129T=	NP_001165949.1:n.49-6129T=
NM_015713.5:c.190T= MANE Select	NP_056528.2:p.Trp64=